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Synaptic modifications at the CA3–CA1 synapse after chronic AMPA receptor blockade in rat hippocampal slices

机译:大鼠海马切片中慢性AMPA受体阻滞后CA3-CA1突触的突触修饰

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摘要

Maintenance of dendritic spines, the postsynaptic elements of most glutamatergic synapses in the central nervous system, requires continued activation of AMPA receptors. In organotypic hippocampal slice cultures, chronic blockade of AMPA receptors for 14 days induces a substantial loss of dendritic spines on CA1 pyramidal neurons. Here, using serial section electron microscopy, we show that loss of dendritic spines is paralleled by a significant reduction in synapse density. In contrast, we observed an increased number of asymmetric synapses onto the dendritic shaft, suggesting that spine retraction does not inevitably lead to synapse elimination. Functional analysis of the remaining synapses revealed that hippocampal circuitry compensates for the anatomical loss of synapses by increasing synaptic efficacy. Moreover, we found that the observed morphological and functional changes were associated with altered bidirectional synaptic plasticity. We conclude that continued activation of AMPA receptors is necessary for maintaining structure and function of central glutamatergic synapses.
机译:维持中枢神经系统中大多数谷氨酸能突触的突触后元件树突棘需要持续激活AMPA受体。在器官型海马切片培养物中,AMPA受体的慢性阻滞持续14天会导致CA1锥体神经元上的树突棘大量丧失。在这里,使用串行截面电子显微镜,我们显示出突触密度的显着降低与树突棘的损失平行。相反,我们观察到树突轴上不对称突触的数量增加,这表明脊柱缩回并不能不可避免地导致突触消除。其余突触的功能分析表明,海马回路通过增加突触效力来补偿突触的解剖学损失。此外,我们发现观察到的形态和功能变化与双向突触可塑性改变有关。我们得出结论,AMPA受体的持续激活对于维持中央谷氨酸能突触的结构和功能是必要的。

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